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Geldanamycin | CAS [30562-34-6] | binds HSP90 | anti-tumor activity | A.G.Scien

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产品名称: Geldanamycin | CAS [30562-34-6] | binds HSP90 | anti-tumor activity | A.G.Scien
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简单介绍

CAS:30562-34-6Formula:C29H40N2O9MW:560.6Appearance:YellowSolidPurity:98.4%


Geldanamycin | CAS [30562-34-6] | binds HSP90 | anti-tumor activity | A.G.Scien  的详细介绍

Geldanamycin is a benzoquinone ansamycin antibiotic which binds to Hsp90 (Heat Shock Protein 90) and alters it function. HSP90 client proteins play important roles in the regulation of the cell cycle, cell growth, cell survival, apoptosis, and oncogenesis.Cdc28 provides a molecular link between Hsp90, morphogenesis, and cell cycle progression inCandida albicans.Epidermal Growth Factor Receptors with Tyrosine Kinase Domain Mutations Exhibit Reduced Cbl Association, Poor Ubiquitylation, and Down-regulation but Are Efficiently Internalized.Inhibition of HSP90 in Trypanosoma cruzi Induces a Stress Response but No Stage Differentiation, Role of the Heat Shock Protein 90 in Immune Response Stimulation by Bacterial DNA and Synthetic Oligonucleotides.

Additional Information

SynonymsGA
Product #G-1047
CAS #30562-34-6
Chemical Name[(3R,5S,6R,7S,8E,10S,11S,12Z,14E)-6-HYDROXY-5,11,21-TRIMETHOXY-3,7,9,15-TETRAMETHYL-16,20,22-TRIOXO-17-AZABICYCLO[16.3.1]DOCOSA-1(21),8,12,14,18-PENTAEN-10-YL] CARBAMATE
FormulaC29H40N2O9
MW560.6
AppearanceYellow Solid
Purity98.4%
SolubilityDMSO: Clear yellow solution at 10 mg/ml, CH2Cl2: Clear yellow solution at 5 mg/ml
Melting Point260°C
Storage Temp-20°C. PROTECT FROM LIGHT!
Therapeutic AreaOncological Disorders
UseGeldanamycin Analogue in Treating Patients With Colon Cancer

Additional Information

MDL NumberMFCD00274570
ChemACXX1035747-8
InChIInChI=1S/C29H40N2O9/c1-15-11-19-25(34)20(14-21(32)27(19)39-7)31-28(35)16(2)9-8-10-22(37-5)26(40-29(30)36)18(4)13-17(3)24(33)23(12-15)38-6/h8-10,13-15,17,22-24,26,33H,11-12H2,1-7H3,(H2,30,36)(H,31,35)/b10-8-,16-9+,18-13+/t15-,17+,22+,23+,24-,26+/m1/s1
SMILESC[C@H]1C[C@@H]([C@@H]([C@H](/C=C(/[C@@H]([C@H](/C=CC=C(C(=O)NC2=CC(=O)C(=C(C1)C2=O)OC)/C)OC)OC(=O)N)C)C)O)OC
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